Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Acute Coronary Syndrome
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This is a mixed-design study. It includes a two-group parallel, randomized clinical trial with acute coronary syndrome patients.Masking: Single (Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 80 years
Gender
Both males and females

Description

So far, there are no previous studies that analyze the effects of neuromuscular training on functional capacity in patients with acute coronary syndrome. Aim: The main objective of this study is to assess the effects of a 10 weeks neuromuscular training vs traditional strength training programme in ...

So far, there are no previous studies that analyze the effects of neuromuscular training on functional capacity in patients with acute coronary syndrome. Aim: The main objective of this study is to assess the effects of a 10 weeks neuromuscular training vs traditional strength training programme in patients with acute coronary syndrome. Design: Randomized clinical trial

Tracking Information

NCT #
NCT04246008
Collaborators
Not Provided
Investigators
Principal Investigator: Maria Dolores Arguisuelas Cardenal Herrera University